SF-1, a key player in adrenal and gonadal differentiation: implications in gonadal dysgenesis and primary ovarian insufficiency

被引:2
作者
Martinerie, L. [1 ]
Bouvattier, C. [2 ]
Lombes, M. [1 ,3 ]
机构
[1] Fac Med Paris Sud 11, INSERM, U693, F-94276 Le Kremlin Bicetre, France
[2] Hop St Vincent de Paul, Assistance Publ Hop Paris, Serv Endocrinol Pediat, F-75014 Paris, France
[3] Hop Bicetre, Assistance Publ Hop Paris, Serv Endocrinol & Malad Reprod, F-94275 Le Kremlin Bicetre, France
关键词
SF1; nuclear receptor; gonadal dysgenesis; primary ovarian insufficiency; STEROIDOGENIC FACTOR-I; XY SEX REVERSAL; NUCLEAR RECEPTOR; CELL-PROLIFERATION; ENZYME EXPRESSION; BINDING DOMAIN; 46; XY PATIENT; NR5A1; MUTATION; DISORDERS;
D O I
10.1016/S0003-4266(09)72473-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Steroidogenic factor 1 (SF-1) gene, identified by Keith Parker in 1992, encodes for an orphan nuclear receptor, NR5A1, whose expression is detected during fetal life in adrenal and gonadal steroidogenic tissues, but also in the developping hypothalamus and in pituitary gonadotropic cells. SF-1 knock-out mouse models exhibit complete adrenal and gonadal agenesis. Human mutations of this transcription factor, were initially associated with primary adrenal failure and male gonadal dysgenesis with various degrees of underandrogenization. More recently, identification of novel SF-l mutations responsible for isolated 46, XY gonadal dysgenesis or 46, XX primary ovarian insufficiency, underscores its central role in the control and maintenance of adrenal and reproductive functions. A better understanding in the regulatory mechanisms of SF-1 signaling pathway, will open new avenues for diagnostic and therapeutic managements of sex differentiation disorders and infertilities. (C) 2009 Elsevier Masson SAS. All rights reserved
引用
收藏
页码:S26 / S32
页数:7
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